Abstract

Schizophrenia is generally considered to be among the most severe psychiatric disorders because of the excessive mortality associated with it. Research to find means to reduce this excessive mortality is warranted. To investigate associations of long-acting injectable antipsychotics (LAIs) with all-cause, natural-cause, and suicide mortality risks as well as the impacts of early use of LAIs in patients with newly diagnosed schizophrenia. This cohort study used data from the Taiwan National Health Insurance Research Database to construct a population-based cohort of patients with schizophrenia who received oral antipsychotics (OAPs) from January 1, 2002, to December 31, 2017. Within this cohort, the LAI group was defined as patients who switched to LAIs and were prescribed LAIs at least 4 times within 1 year. The LAI group was propensity matched 1:1 to patients who continued receiving OAPs of the same compounds. All patients were followed up until switching the antipsychotic administration route, death, or the end of the study (December 31, 2018), whichever occurred first. Data analysis was performed from January 2002 to December 2018. All-cause mortality, natural-cause mortality, suicide mortality, and suicide attempts. In total, 2614 patients who switched to LAIs (median [interquartile range] {IQR} age, 30 [23-39] years) and 2614 who received OAPs (median [IQR] age, 30 [23-39] years) were included (1333 male patients [51.0%] in each group). During the 16-year follow-up period (median [IQR] follow-up of 14 [10-17] years), patients who switched to LAIs had lower risks of all-cause mortality (adjusted hazard ratio [aHR], 0.66; 95% CI, 0.54-0.81), natural-cause mortality (aHR, 0.63; 95% CI, 0.52-0.76), and suicide attempts (incidence rate ratio, 0.72; 95% CI, 0.55-0.93) compared with patients who received the corresponding OAPs. A 47% lower suicide mortality risk (aHR, 0.53; 95% CI, 0.30-0.92) was observed in patients who switched to LAIs within the first 2 years of OAP initiation. These findings suggest that LAI use in patients with newly diagnosed schizophrenia is associated with decreased all-cause mortality and suicide risk. Furthermore, early treatment with LAIs within the first 2 years of OAP initiation was associated with a decrease in suicide mortality risk. Thus, LAI use in the early stage of treatment should be actively considered for patients with newly diagnosed schizophrenia.

Highlights

  • Schizophrenia is generally considered to be among the most severe psychiatric disorders because of the excessive mortality associated with it

  • During the 16-year follow-up period, patients who switched to long-acting injectable antipsychotic (LAI) had lower risks of all-cause mortality, natural-cause mortality, and suicide attempts compared with patients who received the corresponding oral antipsychotics (OAPs)

  • A 47% lower suicide mortality risk was observed in patients who switched to LAIs within the first 2 years of OAP initiation

Read more

Summary

Introduction

Schizophrenia is generally considered to be among the most severe psychiatric disorders because of the excessive mortality associated with it It has consistently been associated with a life expectancy 10 to 25 years shorter than that of the general population.[1,2] In a meta-analysis, Brown et al[3] suggested that schizophrenia is associated with a large increase in suicide mortality and a moderately increased risk of natural-cause mortality. Illness-related risk factors include prior suicide attempts, depressive symptoms, active positive symptoms, and comorbid substance misuse.[4,7] Effective treatment delivery and adherence are vital for suicide prevention in schizophrenia.[4,7] Compared with oral antipsychotics (OAPs), long-acting injectable antipsychotics (LAIs) were reported to improve treatment adherence in patients with schizophrenia.[8,9] studies of LAIs in protecting against suicide are limited; in particular, the association of LAIs with the course of the illness, if administered at an early phase, remains unclear

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.